Canonical Allele Identifier: CA1300458886

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325797C= , CM000664.2:g.156325797C=	GRCh38
NC_000002.11:g.157182309C= , CM000664.1:g.157182309C=	GRCh37
NC_000002.10:g.156890555C=	NCBI36
NG_011821.1:g.11979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1540G=	ENSP00000514865.1:p.Val514=
ENST00000700229.1:c.708G=
ENST00000700230.1:c.1284G=	ENSP00000514867.1:n.1284G=
ENST00000700231.1:c.1669G=	ENSP00000514868.1:p.Val557=
ENST00000339562.9:c.1744G= MANE Select	ENSP00000344479.4:p.Val582=
ENST00000675870.1:c.*255G=	ENSP00000502739.1:n.*255G=
ENST00000339562.8:c.1744G=	ENSP00000344479.4:p.Val582=
ENST00000409108.6:c.1640G=	ENSP00000386993.2:p.Gly547=
ENST00000409572.5:c.1744G=	ENSP00000386747.1:p.Val582=
ENST00000417764.5:c.*255G=	ENSP00000415632.1:n.*255G=
ENST00000417972.5:c.*255G=	ENSP00000394671.1:n.*255G=
ENST00000426264.5:c.1555G=	ENSP00000389986.1:p.Val519=
ENST00000429376.5:c.1451G=	ENSP00000410952.1:p.Gly484=
NM_006186.3:c.1744G=	NP_006177.1:p.Val582=
XM_005246621.2:c.1777G=	XP_005246678.1:p.Val593=
XM_005246622.2:c.1555G=	XP_005246679.1:p.Val519=
XM_005246623.1:c.1555G=	XP_005246680.1:p.Val519=
XM_006712553.2:c.1702G=	XP_006712616.1:p.Val568=
XM_011511246.1:c.1673G=	XP_011509548.1:p.Gly558=
NM_173173.2:c.1555G=	NP_775265.1:p.Val519=
XM_005246621.4:c.1777G=	XP_005246678.1:p.Val593=
XM_006712553.4:c.1702G=	XP_006712616.1:p.Val568=
XM_011511246.2:c.1673G=	XP_011509548.1:p.Gly558=
XM_017004219.2:c.1744G=	XP_016859708.1:p.Val582=
XM_017004220.2:c.1669G=	XP_016859709.1:p.Val557=
XR_001738751.2:n.1991G=
XR_001738752.2:n.1813G=
XR_427087.4:n.1870G=
NM_006186.4:c.1744G= MANE Select	NP_006177.1:p.Val582=
NM_173173.3:c.1555G=	NP_775265.1:p.Val519=